JPH0687787B2 - How to make salad oil - Google Patents

How to make salad oil

Info

Publication number
JPH0687787B2
JPH0687787B2 JP2327113A JP32711390A JPH0687787B2 JP H0687787 B2 JPH0687787 B2 JP H0687787B2 JP 2327113 A JP2327113 A JP 2327113A JP 32711390 A JP32711390 A JP 32711390A JP H0687787 B2 JPH0687787 B2 JP H0687787B2
Authority
JP
Japan
Prior art keywords
oil
liquid
weight
palm
present
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Lifetime
Application number
JP2327113A
Other languages
Japanese (ja)
Other versions
JPH04197188A (en
Inventor
幸一 田村
信夫 田口
敏 田代
Original Assignee
日清製油株式会社
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by 日清製油株式会社 filed Critical 日清製油株式会社
Priority to JP2327113A priority Critical patent/JPH0687787B2/en
Priority to US07/727,445 priority patent/US5183675A/en
Priority to MYPI91001240A priority patent/MY105499A/en
Priority to GB9115101A priority patent/GB2250299B/en
Priority to DE4125415A priority patent/DE4125415A1/en
Publication of JPH04197188A publication Critical patent/JPH04197188A/en
Publication of JPH0687787B2 publication Critical patent/JPH0687787B2/en
Priority to SG180494A priority patent/SG180494G/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • AHUMAN NECESSITIES
    • A23FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
    • A23DEDIBLE OILS OR FATS, e.g. MARGARINES, SHORTENINGS, COOKING OILS
    • A23D9/00Other edible oils or fats, e.g. shortenings, cooking oils
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11CFATTY ACIDS FROM FATS, OILS OR WAXES; CANDLES; FATS, OILS OR FATTY ACIDS BY CHEMICAL MODIFICATION OF FATS, OILS, OR FATTY ACIDS OBTAINED THEREFROM
    • C11C3/00Fats, oils, or fatty acids by chemical modification of fats, oils, or fatty acids obtained therefrom
    • C11C3/04Fats, oils, or fatty acids by chemical modification of fats, oils, or fatty acids obtained therefrom by esterification of fats or fatty oils
    • C11C3/10Ester interchange

Description

【発明の詳細な説明】 〔産業上の利用分野〕 本発明は、パーム油を処理して得られる特定の油脂を原
料として、有用な液体油であるサラダ油を製造する方法
に関する。
Description: TECHNICAL FIELD The present invention relates to a method for producing a useful liquid oil, salad oil, using a specific fat or oil obtained by treating palm oil as a raw material.

〔従来の技術〕[Conventional technology]

常温で固体を呈する固体脂は、使用上の不便であるた
め、これを液体油に変換することが普通行なわれてい
る。パーム油のような固体脂は近年大量に生産され、し
かも今後増加することが予想されており、そのためそれ
らの新規かつ有用な用途の開発が強く望まれている。し
かしながら、固体脂のままでは、それらの用途におのず
から限度がある。そこでこのような観点から固体脂であ
るパーム油から液体のサラダ油を製造することができれ
ば極めて有意義であることは、言うまでもない。
Since solid fat which is solid at room temperature is inconvenient to use, it is usually converted to liquid oil. Solid fats such as palm oil have been produced in large quantities in recent years, and are expected to increase in the future. Therefore, development of new and useful uses thereof is strongly desired. However, if the solid fat is used as it is, there is a limit in its use. From this point of view, it goes without saying that it would be extremely meaningful if liquid salad oil can be produced from palm oil, which is a solid fat.

一般的に固体脂を液体化しようとする試みは従来から色
々行なわれてきた。最も簡単な方法は、単に固体脂を液
体油と配合することであるが、所望の液体油とするには
固体脂の配合可能量が極めて少量に限定され、それ故有
効な手段ということができないものであった。
In general, various attempts have been made to liquefy solid fats. The simplest method is simply to blend the solid fat with the liquid oil, but the amount of the solid fat that can be blended is limited to a very small amount in order to obtain the desired liquid oil, and therefore it cannot be said to be an effective means. It was a thing.

また固体脂を分別して低融点部を取得する方法が知られ
ているが、パーム油の分別オレインの例でも明らかなよ
うに、低融点部といえども夏季以外は、固形を呈する傾
向があり、そのためせいぜい半液体油と言える程度のも
のが得られるにすぎなかった。
Also known is a method of obtaining a low melting point portion by separating the solid fat, but as is clear in the example of the fractionated olein of palm oil, even in the low melting point portion, except during summer, there is a tendency to present a solid, Therefore, at most, it was possible to obtain a semi-liquid oil.

前述の如き事情に鑑み、近年リパーゼを用いるエステル
交換反応に基く方法が各種提案されている。例えば特開
昭61-293389公報には、パーム油と、無臭の液状原料油
とをリパーゼを用いて1,3特異性のあるエステル交換を
行うことが開示されているが、パーム油の配合量が50%
どまりであり、必ずしも満足すべき方法とはいえない。
In view of the above-mentioned circumstances, various methods based on a transesterification reaction using lipase have recently been proposed. For example, JP-A-61-293389 discloses that palm oil and odorless liquid raw material oil are transesterified with 1,3 specificity using a lipase. Is 50%
It's a stoppage and not always a satisfactory method.

一方、特開昭49-107304公報及び特開昭64-81899公報に
はパーム分別油に液状油を配合し、エステル交換する方
法が述べられているが、得られる油脂の耐冷却性は不十
分である。
On the other hand, JP-A-49-107304 and JP-A-64-81899 describe a method of blending a liquid oil with a palm fractionated oil and transesterifying the oil, but the resulting oil has insufficient cooling resistance. Is.

〔発明が解決しようとする課題〕[Problems to be Solved by the Invention]

本発明の目的は、前記問題を生ずることなく、固体脂で
あるパーム油から効率よくサラダ油を製造する方法を提
供することにある。
An object of the present invention is to provide a method for efficiently producing salad oil from palm oil, which is a solid fat, without causing the above problems.

〔課題を解決するための手段〕[Means for Solving the Problems]

本発明は、パーム油を処理して特定の特性を有する油脂
とし、これを別の組成の液体食用油と均一に混合した
後、上記油脂を構成する脂肪酸残基と液体食用油を構造
する脂肪酸残基との間で1,3特異的エステル交換を行な
わせると、サラダ油を効率的に製造でき、上記課題を効
率よく達成できるとの知見に基づいて達成されたのであ
る。
The present invention processes palm oil into an oil and fat having specific properties, and after uniformly mixing this with a liquid edible oil having a different composition, a fatty acid residue that constitutes the above oil and fat and a fatty acid that constitutes the liquid edible oil. This was accomplished based on the finding that 1,3-specific transesterification with residues allows salad oil to be efficiently produced and the above-mentioned objects to be efficiently achieved.

すなわち、本発明は、(A)パーム油を原料とする下記
特性を有する油脂: 沃素価 55〜75 構成脂肪酸組成 パルミチン酸30〜42重量% オレイン酸 42〜48重量% リノール酸 11〜20重量% トリパルミチン 2重量%以下 上昇融点 5〜25℃ と(B)成分(A)以外の液状食用油との5:95〜95:5
(重量比)である混合物を、1,3特異性を有する固定化
リパーゼを用いて無溶媒下でエステル交換し、次いで生
成物を無溶媒下で分画することを特徴とするサラダ油の
製造方法を提供する。
That is, the present invention uses (A) palm oil as a raw material having the following characteristics: iodine value 55 to 75 constituent fatty acid composition palmitic acid 30 to 42% by weight oleic acid 42 to 48% by weight linoleic acid 11 to 20% by weight Tripalmitin 2% by weight or less 5:95 to 95: 5 with melting point 5 to 25 ° C and liquid edible oil other than component (A) (A)
A method for producing a salad oil, which comprises transesterifying a mixture (weight ratio) using immobilized lipase having 1,3 specificity in the absence of a solvent, and then fractionating the product in the absence of the solvent. I will provide a.

上記特性を有する成分(A)の油脂としては、特に沃素
価が57〜75、パルミチン酸残基の量が30〜40重量%(以
下%と略称する。)、上昇融点5〜25℃のものが好まし
い。本発明で用いる成分(A)の油脂は、パーム油を原
料とし、これを乾式分別法や溶剤分別法などにより、か
つ処理条件を上記の特性が得られるように調整すること
によって得られる。本発明は上記特性の油脂を用いるこ
とが重要であり、上記範囲をはずれた原料油では所期の
目的を達することができない。
As the oil and fat of the component (A) having the above characteristics, those having an iodine value of 57 to 75, a palmitic acid residue amount of 30 to 40% by weight (hereinafter abbreviated as%), and a rising melting point of 5 to 25 ° C. Is preferred. The oil and fat of the component (A) used in the present invention is obtained by using palm oil as a raw material, and subjecting this to a dry fractionation method, a solvent fractionation method and the like, and adjusting the treatment conditions so as to obtain the above characteristics. In the present invention, it is important to use oils and fats having the above-mentioned characteristics, and a raw material oil outside the above range cannot achieve the intended purpose.

なお、上記の沃素価、脂肪酸組成および上昇融点は基準
油脂分析法(油化学協会編)により、又パルミチン量は
高速液体クロマトグラフィーによる数値である。
The iodine value, the fatty acid composition and the rising melting point are based on the standard oil and fat analysis method (edited by Japan Oil Chemistry Association), and the amount of palmitin is based on high performance liquid chromatography.

本発明で用いる1,3特異性を有する固定化リパーゼとし
ては、例えばノポ社のリポザイムをあげることができ
る。このものはムコールミーハイ(Mucor Miehei)由来
の1,3特異性を有するリパーゼを、イオン交換樹脂を担
体として固定化したものである。尚、本発明で用いる固
定化リパーゼは、これに限定されるものではなく、1,3
特異性を有するリパーゼを公知の担体に担持させたもの
であればいずれも使用することができる。
Examples of the immobilized lipase having 1,3 specificity used in the present invention include lipozymes manufactured by Nopo. This is a product in which a lipase having 1,3 specificity derived from Mucor Miehei is immobilized using an ion exchange resin as a carrier. The immobilized lipase used in the present invention is not limited to this, and 1,3
Any lipase having specificity supported on a known carrier can be used.

本発明で成分(B)として用いる液体食用油としては、
大豆油、菜種油、綿実油、コーン油、サフラワー油、米
油、ヒマワリ油、ゴマ油等の1種又は2種以上の混合物
を挙げることができる。
The liquid edible oil used as the component (B) in the present invention includes:
Examples include soybean oil, rapeseed oil, cottonseed oil, corn oil, safflower oil, rice oil, sunflower oil, sesame oil, and the like, or a mixture of two or more thereof.

更に、本発明で用いる両油成分は、脱酸油、脱色油、脱
臭油のいずれでもよい。また本発明で用いる成分(A)
の油脂と成分(B)の液体食用油の配合割合(重量比)
は、本発明の目的がサラダ油としての規格(日本農林規
格で、0℃で5.5時間くもりを生じない)を満足する耐
冷却性を有する液体油の製造にあることから、5〜95:9
5〜5、好ましくは55〜90:45〜10の割合とするのがよ
い。
Further, both oil components used in the present invention may be any of deoxidized oil, decolorized oil and deodorized oil. Further, the component (A) used in the present invention
Mixing ratio (weight ratio) of oils and fats and liquid edible oil of component (B)
Since the object of the present invention is to produce a liquid oil having cooling resistance which satisfies the standard as a salad oil (Japanese agricultural standard, no cloudiness occurs at 0 ° C for 5.5 hours), 5 to 95: 9
The ratio is 5 to 5, preferably 55 to 90:45 to 10.

上記配合割合の混合物をエステル交換することによっ
て、実用的経済性を保ち、かつ十分に満足し得る収率を
もってサラダ油を製造することができるのである。
By transesterifying the mixture having the above blending ratio, it is possible to produce a salad oil with a practically satisfactory yield and a sufficiently satisfactory yield.

すなわち、液体食用油5に対するパーム油脂の量が95を
越える混合物を原料として使用すると、後の分画工程に
おいて満足し得る収率をもってサラダ油を回収すること
はできない。尚、液体食用油45に対する油脂の量が55以
上であるとより経済的にサラダ油を製造することができ
る。
That is, when a mixture containing palm oil and fat in an amount of more than 95 relative to the liquid edible oil 5 is used as a raw material, the salad oil cannot be recovered with a satisfactory yield in the subsequent fractionation step. If the amount of fats and oils relative to the liquid edible oil 45 is 55 or more, the salad oil can be produced more economically.

本発明のエステル交換反応は、約60〜80℃特に約70℃近
辺で行なうのがよい。
The transesterification reaction of the present invention is preferably carried out at about 60 to 80 ° C, particularly about 70 ° C.

反応(エステル交換反応)速度を高めるためには常識的
に、高温であることが望ましい。しかしながら余り高い
と失活の問題が生ずるおそれがある。
In order to increase the reaction (transesterification) rate, it is common sense that the temperature is high. However, if it is too high, the problem of deactivation may occur.

本発明に於てはまた油の均一混合物は、反応温度に於て
飽和の、水を含むように調整することが望ましい。
In the present invention, it is also desirable to prepare the homogeneous mixture of oils to contain water which is saturated at the reaction temperature.

このようにすると、反応中に副生する遊離脂肪酸含量を
低く抑えることができ、かつ固定化リパーゼの活性を極
めて長時間にわたり維持することができるからである。
This is because the content of free fatty acids by-produced during the reaction can be kept low and the activity of the immobilized lipase can be maintained for an extremely long time.

更に、本発明において、エステル交換は、バッチ方式で
も連続方式でも実施可能である。しかし、固定化リパー
ゼを充填したカラムを用いる連続方式の方が設備及び効
率の観点から得策である。
Further, in the present invention, transesterification can be carried out in a batch system or a continuous system. However, the continuous system using a column packed with immobilized lipase is better from the viewpoint of equipment and efficiency.

すなわち、バッチ方式では反応を十分進行させるため、
とくに固体脂では比較的高温で長時間加温しなければな
らず、かつ副反応として起る加水分解により生成する遊
離脂肪酸の量が多くなるが、連続方式によれば加温時間
が短くて済み、かつ副生脂肪酸の量も低く抑えられるか
らである。
That is, in the batch system, to allow the reaction to proceed sufficiently,
In particular, solid fat must be heated at a relatively high temperature for a long time, and the amount of free fatty acids produced by hydrolysis that occurs as a side reaction increases, but the continuous method requires a short heating time. In addition, the amount of by-produced fatty acids can be suppressed to a low level.

本発明に於ては、さらにこのようにして製造された改質
生成物から固体脂分を分画により分離する。
In the present invention, solid fat is further separated from the modified product thus produced by fractionation.

分画は無溶媒下で行なう。このように無溶媒で行なうこ
とは本発明の特長の1つである。本発明の目的生成物で
あるサラダ油(日本農林規格では0℃で5.5時間くもり
を生じない)を得るには3〜10℃、好ましくは約5℃ま
でに時間をかけて冷却し反応物中の固形成分を析出さ
せ、常法により固体脂分を濾過分画する。
Fractionation is performed without solvent. Thus, carrying out without a solvent is one of the features of the present invention. In order to obtain the desired product of the present invention, which is a salad oil (it does not cause cloudy weather at 0 ° C for 5.5 hours according to Japanese Agricultural Standards), the reaction mixture is cooled to 3 to 10 ° C, preferably about 5 ° C over a period of time. The solid component is deposited and the solid fat is filtered and fractionated by a conventional method.

〔発明の効果〕〔The invention's effect〕

本発明によれば、従来法に比べてパーム油由来の原料の
配合量を多くでき、しかも満足すべき耐冷却性を有する
サラダ油を製造することができる。
According to the present invention, it is possible to produce a salad oil having a larger amount of the raw material derived from palm oil than that of the conventional method and having satisfactory cooling resistance.

次に本発明を実施例により説明する。Next, the present invention will be described with reference to examples.

〔実施例〕〔Example〕

実施例1 パーム油を乾式分別法で処理して得られた沃素価58.0、
パルミチン酸39.8%、オレイン酸42..5%、リノール酸1
1.2%、トリパルミチン0.2%、融点21.6℃の油脂40%、
菜種油60%を均一に混合し、65℃で固定化リパーゼ「リ
ポザイム」(ノボ社製)を300g充填した1のカラムに
毎時360gの流量で通液してエステル交換を行った。初期
72時間までの反応物をカットし、そのあとの反応物を5k
gほど得、乾燥後5℃まで48時間かけて徐冷し、析出し
た結晶を同温度まで濾別した。液体油歩留は87%で、液
体油を0℃氷水中で冷却したところ、30時間でもくもり
を生じず、サラダ油としての耐冷却性を十分に備えてい
た。
Example 1 Palm oil was treated by a dry fractionation method to obtain an iodine value of 58.0,
Palmitic acid 39.8%, oleic acid 42.5%, linoleic acid 1
1.2%, tripalmitin 0.2%, melting point 21.6 ° C oil 40%,
60% of rapeseed oil was uniformly mixed, and transesterification was performed at 65 ° C. by passing it through one column packed with 300 g of immobilized lipase “lipozyme” (manufactured by Novo) at a flow rate of 360 g per hour. initial
Cut the reaction product up to 72 hours, and the subsequent reaction product 5k
About g was obtained, and after drying, the mixture was gradually cooled to 5 ° C. over 48 hours, and the precipitated crystals were filtered to the same temperature. The liquid oil yield was 87%, and when the liquid oil was cooled in ice water at 0 ° C., cloudiness did not occur even after 30 hours, and it had sufficient cooling resistance as salad oil.

比較例1 沃素価52.1、パルミチン酸44.0%、オレイン酸39.2%、
リノール酸10.2%、トリパルミチン9.4%、融点35℃の
パーム油40%、菜種油(実施例1と同じもの)60%を均
一に混合し、実施例1と同様にエステル交換及び徐冷を
行った。液体油歩留は78%で、実施例1と同様に冷却し
たところ17時間で、くもりを生じた。
Comparative Example 1 Iodine value 52.1, Palmitic acid 44.0%, Oleic acid 39.2%,
Linoleic acid 10.2%, tripalmitin 9.4%, palm oil 40% with a melting point of 35 ° C., and rapeseed oil (the same as in Example 1) 60% were uniformly mixed, and transesterification and slow cooling were performed in the same manner as in Example 1. . The liquid oil yield was 78%, and when cooled in the same manner as in Example 1, cloudiness occurred in 17 hours.

比較例2 実施例1のパーム処理油40%、菜種油60%を均一に混合
した後5℃まで48時間かけて徐冷し、同温度で濾別し
た。液体歩留は58%で、実施例1の場合に比べ、大巾に
低く、実用性に乏しかった。
Comparative Example 2 40% of the palm-treated oil of Example 1 and 60% of rapeseed oil were uniformly mixed, then gradually cooled to 5 ° C over 48 hours, and filtered at the same temperature. The liquid yield was 58%, which was much lower than that of Example 1 and was poor in practicality.

実施例2 実施例1で用いたのと同じパーム処理油60%、菜種油40
%を均一に混合し、65℃で固定化リパーゼ「リポザイ
ム」(ノボ社製)を300g充填した1のカラムに毎時36
0gの流量で通液してエステル交換を行った。初期72時ま
での反応物をカットし、そのあとの反応物を5kgほど
得、乾燥後5℃まで48時間かけて徐冷し、析出した結晶
を同温度で濾別した。液体油歩留は70%で、液体油を0
℃の氷水中で冷却したところ5.5時間でくもりを生じ
ず、サラダ油としての耐冷却性を備えていた。
Example 2 The same palm treated oil used in Example 1 60%, rapeseed oil 40
% Evenly mixed, and at 65 ° C., one column packed with 300 g of immobilized lipase “lipozyme” (manufactured by Novo Co.) at 36 ° C. per hour
The liquid was passed through at a flow rate of 0 g for transesterification. The reaction product up to 72 o'clock in the initial stage was cut, and about 5 kg of the reaction product was obtained, dried and then gradually cooled to 5 ° C. over 48 hours, and the precipitated crystal was separated by filtration at the same temperature. Liquid oil yield is 70% and liquid oil is 0
When it was cooled in ice water at ℃, it did not fog in 5.5 hours and had cooling resistance as salad oil.

比較例3 実施例1で用いたのと同じパーム処理油60%、菜種油40
%を均一に混合し、次いで5℃まで48時間冷却したとこ
ろ、液体油を濾別することができなかった。
Comparative Example 3 The same palm processed oil as used in Example 1 60%, rapeseed oil 40
% Was mixed homogeneously and then cooled to 5 ° C. for 48 hours, the liquid oil could not be filtered off.

実施例3 実施例1で用いたのと同じパーム処理油40%と大豆油60
%を均一に混合し、実施例1と同一条件にてエステル交
換、分画し、液体部の冷却を行った。その結果、液体油
歩留は84%で液体油を0℃の氷水中で冷却したところ5.
5時間以上曇りを生じなかった。
Example 3 The same palm processed oil 40% and soybean oil 60 used in Example 1
% Were uniformly mixed, transesterification and fractionation were carried out under the same conditions as in Example 1, and the liquid part was cooled. As a result, the liquid oil yield was 84% and the liquid oil was cooled in 0 ° C ice water.
No clouding occurred for more than 5 hours.

実施例4 実施例1で用いたのと同じパーム処理油40%、コーン油
60%を均一に混合し、実施例1と同一条件にてエステル
交換、分画し、液体部の冷却を行った。その結果、液体
油歩留は85%で液体油を0℃の氷水中で冷却したところ
5.5時間以上曇りを生じなかった。
Example 4 The same palm processed oil 40%, corn oil used in Example 1
60% was uniformly mixed, transesterification and fractionation were carried out under the same conditions as in Example 1, and the liquid part was cooled. As a result, the liquid oil yield was 85% and the liquid oil was cooled in ice water at 0 ° C.
No cloudiness occurred for more than 5.5 hours.

比較例4 実施例3と同一配合の油脂をエステル交換せずに実施例
1と同一条件で分画した。液体油の歩留は59%であっ
た。
Comparative Example 4 Oils and fats having the same composition as in Example 3 were fractionated under the same conditions as in Example 1 without transesterification. The liquid oil yield was 59%.

比較例5 実施例4と同一配合の油脂をエステル交換せずに実施例
1と同一条件で分画した。液体油の歩留は55%であっ
た。
Comparative Example 5 Oils and fats having the same composition as in Example 4 were fractionated under the same conditions as in Example 1 without transesterification. The liquid oil yield was 55%.

Claims (1)

【特許請求の範囲】[Claims] 【請求項1】(A)パーム油を原料とする下記特性を有
する油脂: 沃素価 55〜75 構成脂肪酸組成 パルミチン酸30〜42重量% オレイン酸 42〜48重量% リノール酸 11〜20重量% トリパルミチン 2重量%以下 上昇融点 5〜25℃ と(B)成分(A)以外の液状食用油との5:95〜95:5
(重量比)である混合物を、1,3特異性を有する固定化
リパーゼを用いて無溶媒下でエステル交換し、次いで生
成物を無溶媒下で分画することを特徴とするサラダ油の
製造方法。
1. (A) Oil and fat made from palm oil and having the following characteristics: iodine value 55 to 75 constituent fatty acid composition palmitic acid 30 to 42% by weight oleic acid 42 to 48% by weight linoleic acid 11 to 20% by weight Palmitin 2% by weight or less 5:95 to 95: 5 with melting point 5 to 25 ° C and liquid edible oil other than component (A) (B)
A method for producing a salad oil, which comprises transesterifying a mixture (weight ratio) using immobilized lipase having 1,3 specificity in the absence of a solvent, and then fractionating the product in the absence of the solvent. .
JP2327113A 1990-11-28 1990-11-28 How to make salad oil Expired - Lifetime JPH0687787B2 (en)

Priority Applications (6)

Application Number Priority Date Filing Date Title
JP2327113A JPH0687787B2 (en) 1990-11-28 1990-11-28 How to make salad oil
US07/727,445 US5183675A (en) 1990-11-28 1991-07-09 Process for producing salad oil
MYPI91001240A MY105499A (en) 1990-11-28 1991-07-10 Process for producing salad oil.
GB9115101A GB2250299B (en) 1990-11-28 1991-07-12 Process for producing salad oil
DE4125415A DE4125415A1 (en) 1990-11-28 1991-07-31 METHOD FOR THE PRODUCTION OF SALAD OIL
SG180494A SG180494G (en) 1990-11-28 1994-12-29 Process for producing salad oil

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP2327113A JPH0687787B2 (en) 1990-11-28 1990-11-28 How to make salad oil

Publications (2)

Publication Number Publication Date
JPH04197188A JPH04197188A (en) 1992-07-16
JPH0687787B2 true JPH0687787B2 (en) 1994-11-09

Family

ID=18195444

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2327113A Expired - Lifetime JPH0687787B2 (en) 1990-11-28 1990-11-28 How to make salad oil

Country Status (5)

Country Link
US (1) US5183675A (en)
JP (1) JPH0687787B2 (en)
DE (1) DE4125415A1 (en)
GB (1) GB2250299B (en)
MY (1) MY105499A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
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WO2018155490A1 (en) 2017-02-23 2018-08-30 不二製油グループ本社株式会社 Shea olein and method for preparing same

Families Citing this family (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5601860A (en) * 1990-11-30 1997-02-11 American Home Products Corporation Corandomized fat compositions for infant formulas
US6058633A (en) * 1997-10-22 2000-05-09 Barden; William Mark Quick coupling device and method utilizing an over-center spring
CN100339016C (en) * 2003-08-07 2007-09-26 郭兴田 Health-care edible oil of semen sesami nigrum and black soybean and its preparing method
AU2003296865A1 (en) * 2003-12-31 2005-07-21 Council Of Scientific And Industrial Research Process for preparation of homogeneous blended oil
JP4410699B2 (en) * 2005-02-23 2010-02-03 日清オイリオグループ株式会社 Oil and fat composition and method for producing oil and fat composition
JP5161465B2 (en) * 2007-02-15 2013-03-13 株式会社J−オイルミルズ Method for producing highly liquid palm oil and highly liquid palm oil
KR100888225B1 (en) 2007-07-03 2009-03-12 주식회사농심 Structured Lipids reduced of Saturated Lipids

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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AU540882B2 (en) * 1980-03-08 1984-12-06 Fuji Oil Company Limited Enzymatic transesterification of lipid and enzyme used therein
US4420560A (en) * 1981-11-17 1983-12-13 Fuji Oil Company, Limited Method for modification of fats and oils
JPS61293389A (en) * 1985-06-19 1986-12-24 Nisshin Oil Mills Ltd:The Production of salad oil
JP2687337B2 (en) * 1987-02-13 1997-12-08 味の素株式会社 Liquid oil manufacturing method
JPH10293389A (en) * 1997-04-18 1998-11-04 Puritetsuku:Kk Printer, printing method, control method for printer and recording medium

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2018155490A1 (en) 2017-02-23 2018-08-30 不二製油グループ本社株式会社 Shea olein and method for preparing same

Also Published As

Publication number Publication date
GB2250299B (en) 1994-10-12
US5183675A (en) 1993-02-02
DE4125415A1 (en) 1992-06-04
JPH04197188A (en) 1992-07-16
GB2250299A (en) 1992-06-03
GB9115101D0 (en) 1991-08-28
MY105499A (en) 1994-10-31

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